Chlorhexidine Gluconate Solution 0.75% Antiseptic Solution
Product Images NDC 61037-414

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Chlorhexidine Gluconate Solution 0.75% Antiseptic (NDC 61037-414). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bajaj Medical, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Lbl1200ml

Drug Facts panels for Chlorhexidine Gluconate Solution 0.75% Antiseptic by Bajaj Medical, LLC. The panels detail active ingredient concentration, purpose as antiseptic, usage instructions for healthcare personnel handwash, warnings including allergy alerts, directions, storage conditions, and a list of inactive ingredients. A contact number for questions is also provided.*

FDA Label Image

Lbl128oz

Label for Chlorhexidine Gluconate Solution 0.75% Antiseptic topical solution, 128 fl oz (3785 mL) by Bajaj Medical, LLC. The label includes drug facts with active ingredient concentration, usage directions, warnings, inactive ingredients, and contact information. The label features FDA approved and Made in USA logos, and a barcode.*

FDA Label Image

Lbl16oz

Chlorhexidine Gluconate Solution 0.75% Antiseptic topical solution in a 16 fl oz (473 mL) bottle. Labeled for external use only, manufactured by Bajaj Medical, LLC. The label includes Drug Facts with active ingredient, purpose, use, warnings, directions, and other information. The NDC number 61037-414 is visible along with an FDA approval symbol and a barcode.*

FDA Label Image

Lbl32oz

Label for Chlorhexidine Gluconate Solution 0.75% Antiseptic topical solution by Bajaj Medical, LLC, Chicago IL. The front displays the concentration 0.75%, usage as an antiseptic, FDA approval, and volume of 32 fl oz (946 mL). The label includes Drug Facts with active ingredient chlorhexidine gluconate solution 0.75%, purpose as antiseptic, use instructions for healthcare personnel handwash, warnings, directions, other information, and inactive ingredients. A barcode is shown at the bottom.*

FDA Label Image

Lbl4oz

Label for Chlorhexidine Gluconate Solution 0.75% Antiseptic solution, topical use, containing 4 fluid ounces (118 mL). The label features the product name prominently with the concentration 0.75%, indicates it is an antiseptic for external use only, and lists Bajaj Medical, LLC, Chicago, IL as the labeler. Includes a barcode and marks the product as made in the USA and FDA approved.*

FDA Label Image

Lbl8oz

Label for Chlorhexidine Gluconate Solution 0.75% Antiseptic, topical solution, 8 fl oz (236 mL) from Bajaj Medical, LLC. The label shows the active ingredient concentration and indicates FDA approval. It includes Drug Facts with usage for healthcare personnel handwash, warnings, directions, inactive ingredients, storage instructions, and a contact number for questions or comments.*

FDA Label Image

Lbl8ozclr

Label for Chlorhexidine Gluconate Solution 0.75% Antiseptic topical solution by Bajaj Medical, LLC. The label highlights the antiseptic strength as 0.75%, indicates FDA approval, and states the volume as 8 fl oz (236 mL). It includes detailed Drug Facts covering active ingredients, usage, warnings, directions, other information, and inactive ingredients.*

FDA Label Image

Lbl8ozwht

Label for Chlorhexidine Gluconate Solution 0.75% Antiseptic, an 8 fl oz (236 mL) topical solution by Bajaj Medical, LLC. The label features front branding with strength and usage reminders, plus detailed Drug Facts panels outlining active ingredient, purpose, usage warnings, allergy alert, directions, storage information, inactive ingredients, and contact details for questions or comments.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.